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Immune function in autistic children
Lara Stern1, Marie-Josée Francoeur, Marie-Noel Primeau
1Department of Psychiatry, McGill University Health Center-Montreal Children's Hospital, Montreal, Quebec, Canada.
Insights
Most autistic children exhibit normal immune function, indicating routine immunologic testing is generally unnecessary. Investigations should be reserved for cases with a history of recurrent infections.
Area of Science:
- Immunology
- Neurodevelopmental Disorders
- Autism Spectrum Disorder
Background:
- Conflicting reports exist regarding immune system abnormalities in children with autistic spectrum disorders (ASD).
- Limited and inconsistent data necessitate further investigation into the proposed association between ASD and immune dysfunction.
Purpose of the Study:
- To prospectively evaluate the immune function in a cohort of autistic children.
- To investigate the potential link between autistic spectrum disorder and immune system anomalies.
Main Methods:
- Prospective data collection from 24 autistic children referred to an immunology clinic.
- Assessment of clinical history, immunoglobulin levels, specific antibody titers, T- and B-cell counts, T-cell proliferation, and complement studies.
Main Results:
- Most autistic children demonstrated normal immune function, including T-cell function and complement levels.
- Only two patients had abnormal immunoglobulin levels, with one diagnosed with common variable immune deficiency.
- Low antibody titers were observed in 12 patients, primarily due to incomplete vaccination status.
Conclusions:
- The majority of autistic children studied presented with normal immune function.
- Routine immunologic investigations are not recommended for most autistic children.
- Immunologic assessment should be considered selectively for autistic children with a history suggestive of recurrent infections.
Background:
There have been reports that some children with autistic spectrum disorders have abnormal immune function. However, data in this area remain scarce and conflicting.
Objective:
To evaluate the immune function of a series of autistic children in the context of this proposed association.
Methods:
We prospectively collected data on 24 autistic children who, between January 1, 1996, and September 30, 1998, were referred unsolicited to an immunology clinic. We examined the clinical history and evaluated immunoglobulin levels; specific antibody titers to diphtheria, tetanus, and Haemophilus influenzae; T- + B-cell numbers; T-cell proliferation; and complement studies.
Results:
Seven of the 24 children had a history of recurrent infections. Only 2 patients had immunoglobulin levels that were outside the age-adjusted reference ranges, 1 of whom was subsequently diagnosed as having common variable immune deficiency. All the patients had normal in vitro T-cell function and complement study results, and only 2 of 24 patients had subtle derangements in T-cell numbers. Elevated levels of IgE were found in 5 patients, which correlated with a clinical history of atopy. Low diphtheria or tetanus antibody levels were found in 12 patients, but in 11 of these, vaccination status was not up-to-date.
Conclusions:
Most of the autistic children studied had normal immune function, suggesting that routine immunologic investigation is unlikely to be of benefit in most autistic children and should be considered only when there is a history suggestive of recurrent infections.
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